LIGHTSCALPEL LS-4020— 510(k) K213669

Substantially Equivalent

Lightscalpel, Inc.

FDA 510(k) clearance K213669 for LIGHTSCALPEL LS-4020, Substantially Equivalent on 2023-02-15. Applicant: Lightscalpel, Inc..

Clearance details

Applicant: Lightscalpel, Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2021-11-22
Decision date: 2023-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.